Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12035735
rs12035735
LRRC8D
0.700 GeneticVariation GWASCAT NUDT15 codon 139 is the best pharmacogenetic marker for predicting thiopurine-induced severe adverse events in Japanese patients with inflammatory bowel disease: a multicenter study. 29923122

2018
dbSNP: rs10419226
rs10419226
CRTC1
A 0.700 GeneticVariation GWASCAT A genome-wide association study identifies new susceptibility loci for esophageal adenocarcinoma and Barrett's esophagus. 24121790

2013
dbSNP: rs11789015
rs11789015
BARX1
A 0.700 GeneticVariation GWASCAT A genome-wide association study identifies new susceptibility loci for esophageal adenocarcinoma and Barrett's esophagus. 24121790

2013
dbSNP: rs2178146
rs2178146 		A 0.700 GeneticVariation GWASCAT A genome-wide association study identifies new susceptibility loci for esophageal adenocarcinoma and Barrett's esophagus. 24121790

2013
dbSNP: rs2687201
rs2687201 		T 0.700 GeneticVariation GWASCAT A genome-wide association study identifies new susceptibility loci for esophageal adenocarcinoma and Barrett's esophagus. 24121790

2013
dbSNP: rs3784262
rs3784262
ALDH1A2
A 0.700 GeneticVariation GWASCAT A genome-wide association study identifies new susceptibility loci for esophageal adenocarcinoma and Barrett's esophagus. 24121790

2013
dbSNP: rs4800353
rs4800353 		T 0.700 GeneticVariation GWASCAT A genome-wide association study identifies new susceptibility loci for esophageal adenocarcinoma and Barrett's esophagus. 24121790

2013
dbSNP: rs7632500
rs7632500
LOC107986152
C 0.700 GeneticVariation GWASCAT A genome-wide association study identifies new susceptibility loci for esophageal adenocarcinoma and Barrett's esophagus. 24121790

2013
dbSNP: rs398122820
rs398122820
B2M
0.010 GeneticVariation BEFREE In this study, we carried out a cellular and biophysical study on the relationships between the effects of OleA on the aggregation and cell interactions of the D76N β2-microglobulin (D76N b2m) variant associated with a familial form of systemic amyloidosis with progressive bowel dysfunction and extensive visceral amyloid deposits. 29571746

2018
dbSNP: rs13361189
rs13361189 		0.010 GeneticVariation BEFREE The SNP rs13361189 was also found to increase the risk of Crohn's disease clinical sub-phenotype (fibrostricturing behaviour, ileal disease, perianal disease, intestinal resection). 26066377

2015
dbSNP: rs2066845
rs2066845
NOD2
0.010 GeneticVariation BEFREE Gly908arg polymorphisms were more prevalent than WT in UK patients with autoimmune disorders (P = 0·049) or enteropathy (P = 0·049). 20646002

2010
dbSNP: rs1800562
rs1800562
HFE ; LOC108783645
0.010 GeneticVariation BEFREE To report a patient with C282Y homozygocity, depleted body iron and intestinal atrophy caused by celiac disease (CD) who experienced resolution of the enteropathy with subsequent normalization of iron metabolism upon gluten-free diet. 15929194

2005
dbSNP: rs121908377
rs121908377
FOXP2
0.010 GeneticVariation BEFREE A point mutation in the forkhead domain of FOXP2 (R553H) is responsible for a severe speech and language disorder, while a series of missense mutations distributed over the forkhead domain of FOXP3 cause a fatal disorder called IPEX, characterized by immune dysregulation, polyendocrinopathy, and enteropathy. 14997560

2004